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DOI: 10.1055/s-2002-32533
Synthesis of Photo-Crosslinkable Hole-Transport Polymers with Tunable Oxidation Potentials And Their Use In Organic Light-Emitting Diodes
Publication History
Publication Date:
28 June 2002 (online)
Abstract
A series of photo-crosslinkable arylamine-based hole-transport copolymers has been synthesized. The synthetic methodology employed allows for the redox potential of the polymer to be tuned by the incorporation of electron-donating or -withdrawing moieties. Upon exposure to ultraviolet radiation, the polymers become insoluble, as evidenced by UV/Vis absorption spectroscopy, a feature that is useful for the fabrication of multilayer organic light-emitting diodes (OLEDs) by solution processing techniques. OLEDs based on these hole-transport polymers have been fabricated and the performance of the devices has been evaluated. The photo-crosslinking process has been optimized so that it no longer adversely impacts device performance.
Key words
hole-transport agents - photo-crosslinked polymers - organic light-emitting diodes - bis(diarylamino)biphenyls
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Adachi C.Nagai K.Tamoto N. App. Phys. Lett. 1995, 66: 2679 - 2
Tang CW.VanSlyke SA. App. Phys. Lett. 1987, 51: 913 - 3
Burroughes JH.Bradley DDC.Brown AR.Marks RN.Mackay K.Friend RH.Burna PL.Holmes AB. Nature 1990, 347: 539 - 4
Bellmann E.Shaheen SE.Grubbs RH.Marder SR.Kippelen B.Peyghambarian N. Chem. Mater. 1999, 11: 399 - 5
Burrows PE.Gu G.Bulovic V.Shen Z.Forrest SR.Thompson ME. IEEE Trans. Electron Devices 1997, 44: 1188 - 6
Bulovic V.Gu G.Burrows PE.Forrest SR.Thompson ME. Nature 1996, 318: 29 - 7
Allcock HR. Chem. Mater. 1994, 6: 1476 - 8
Li X.-C.Yong T.-M.Gruner J.Holmes AB.Moratti SC.Cacialli F.Friend RH. Synth. Met. 1997, 84: 437 - 9
Bayerl MS.Braig T.Nuyken O.Muller DC.Grob M.Meerholz K. Macromol. Rapid Commun. 1999, 20: 224 - 10
Li W.Wang Q.Cui J.Chou H.Shaheen SE.Jabbour GE.Anderson J.Lee P.Kippelen B.Peyghambarian N.Armstrong NR.Marks TJ. Adv. Mater. 1999, 11: 730 - 11
Langer EM.Liberti P. Polym. Commun. 1991, 32: 453 - 12
Watanabe S.Harachima S.Tsukada N. J. Polym. Sci., Polym. Chem. Ed. 1989, 22: 1033 - 13
Rami Reddy AV.Subramanian K.Krishnasamy V.Ravichandran J. Eur. Polym. J. 1996, 32: 916 - 14
Subramanian K.Krishnasamy V.Nanjundan S.Rami Reddy AV. Eur. Polym. J. 2000, 36: 2343 - 15
Zhang YD.Hreha RD.Marder SR.Jabbour GE.Kippelen B.Peyghambarian N. J. Mater. Chem. 2002, 12: 1703 - 16
Hartwig JF. Angew. Chem. Int. Ed. 1998, 37: 2046 - 17
Hu NX,Ong BS,Xie S,Popovic ZD, andHor AM. inventors; Eur. Pat. Appl. 827367. ; Chem. Abstr. 1998, 128, 223711 - 18
Hansen HC.Olsson R.Croston G.Andersson CM. Bioorg. Med. Chem. Lett. 2000, 21: 2435 - 19
Hsieh CJ.Wu SH.Hsiue GH.Hsu CS.Chain S. J. Polym. Sci., Part A: Polym. Chem. 1994, 32: 1077 - 20
Guram AS.Buchwald SL. J. Am. Chem. Soc. 1994, 116: 7901 - 21
Goodbrand HB.Hu NX. J. Org. Chem. 1999, 64: 670